Kjernekompetansemiljø innen genetisk translasjonsforskning
- Prosjektnummer
- 2005018
- Ansvarlig person
- Dag Undlien
- Institusjon
- Oslo universitetssykehus HF - Ullevål sykehus
- Prosjektkategori
- Fagspes. kjernekomp.miljø
- Helsekategori
- Generic Health Relevance
- Forskningsaktivitet
- 2. Aetiology
Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus.
Genes Immun 2011 Apr;12(3):191-8. Epub 2010 des 23
PMID: 21179112
A Common Haplotype in NAPEPLD Is Associated With Severe Obesity in a Norwegian Population-Based Cohort (the HUNT Study).
Obesity (Silver Spring) 2010 Sep. Epub 2010 sep 30
PMID: 20885390
Designing and implementing sample and data collection for an international genetics study: the Type 1 Diabetes Genetics Consortium (T1DGC).
Clin Trials 2010;7(1 Suppl):S5-S32. Epub 2010 jul 5
PMID: 20603248
CD14 polymorphisms and serum CD14 levels through childhood: a role for gene methylation?
J Allergy Clin Immunol 2010 Jun;125(6):1361-8. Epub 2010 apr 15
PMID: 20398919
FTO genotype and weight gain in obese and normal weight adults from a Norwegian population based cohort (the HUNT study).
Exp Clin Endocrinol Diabetes 2010 Oct;118(9):649-52. Epub 2010 apr 6
PMID: 20373279
An inverse association between history of childhood eczema and subsequent risk of type 1 diabetes that is not likely to be explained by HLA-DQ, PTPN22, or CTLA4 polymorphisms.
Pediatr Diabetes 2010 Sep;11(6):386-93. Epub 2009 nov 4
PMID: 19895409
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis.
Ann Rheum Dis 2010 Aug;69(8):1471-4. Epub 2009 sep 3
PMID: 19734133
Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene.
Acta Ophthalmol 2010 May;88(3):323-8. Epub 2009 jan 30
PMID: 19183411
HLA Dr-Dq haplotypes and the TNFA-308 polymorphism: associations with asthma and allergy.
Allergy 2007 Sep;62(9):991-8.
PMID: 17686102
Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis.
Tissue Antigens 2007 Aug;70(2):110-27.
PMID: 17610416
Eosinophil cationic protein (ECP) polymorphisms and association with asthma, s-ECP levels and related phenotypes.
Allergy 2007 Apr;62(4):429-36.
PMID: 17362255
The relation between size at birth and risk of type 1 diabetes is not influenced by adjustment for the insulin gene (-23HphI) polymorphism or HLA-DQ genotype.
Diabetologia 2006 Sep;49(9):2068-73. Epub 2006 mai 12
PMID: 16691379
[Genetic causes of obesity]
Tidsskr Nor Laegeforen 2005 Nov;125(22):3090-3.
PMID: 16299561
[Molecular diagnostics in diabetes mellitus]
Tidsskr Nor Laegeforen 2005 Nov;125(21):2968-72.
PMID: 16276383
Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes.
BMC Genet 2005;6(1):9. Epub 2005 feb 18
PMID: 15720714
CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases.
Pigment Cell Res 2005 Feb;18(1):55-8.
PMID: 15649153
Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes.
Diabetes 2004 Oct;53(10):2709-12.
PMID: 15448105
Association analysis of the lymphocyte-specific protein tyrosine kinase (LCK) gene in type 1 diabetes.
Diabetes 2004 Sep;53(9):2479-82.
PMID: 15331563
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease.
J Clin Endocrinol Metab 2004 Jul;89(7):3474-6.
PMID: 15240634
Remapping the insulin gene/IDDM2 locus in type 1 diabetes.
Diabetes 2004 Jul;53(7):1884-9.
PMID: 15220214
Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene.
Hum Mol Genet 2004 Aug;13(15):1633-9. Epub 2004 jun 2
PMID: 15175274
Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease.
Genes Immun 2004 Aug;5(5):381-8.
PMID: 15164102
Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes.
Diabetes 2004 Apr;53(4):1158-61.
PMID: 15047635
Analysis of the type 2 diabetes-associated single nucleotide polymorphisms in the genes IRS1, KCNJ11, and PPARG2 in type 1 diabetes.
Diabetes 2004 Mar;53(3):870-3.
PMID: 14988278
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease.
Eur J Hum Genet 2008 Aug;16(8):977-82. Epub 2008 feb 27
PMID: 18301444
Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes.
Diabetologia 2008 Apr;51(4):589-96. Epub 2008 feb 22
PMID: 18292987
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.
Diabetes 2008 Apr;57(4):1131-5. Epub 2008 jan 11
PMID: 18192540
T cell-specific T-box transcription factor haplotype is associated with allergic asthma in children.
J Allergy Clin Immunol 2008 Jan;121(1):51-6. Epub 2007 okt 18
PMID: 17949803
Rapid and efficient FBN1 mutation detection using automated sample preparation and direct sequencing as the primary strategy.
Genet Test 2006;10(4):258-64.
PMID: 17253931
The DNA database search controversy revisited: bridging the Bayesian-frequentist gap.
Biometrics 2007 Sep;63(3):922-5.
PMID: 17825021
[Nuts and bolts of percentiles]
Tidsskr Nor Laegeforen 2007 Mar;127(6):733-4.
PMID: 17363985
DNA-testing for immigration cases: the risk of erroneous conclusions.
Forensic Sci Int 2007 Oct;172(2-3):144-9. Epub 2007 feb 20
PMID: 17317060
Prenatal diagnosis of congenital malformations and parental psychological distress--a prospective longitudinal cohort study.
Prenat Diagn 2006 Nov;26(11):1001-9.
PMID: 16958144
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
Am J Hum Genet 2008 Apr;82(4):1003-10. Epub 2008 mar 13
PMID: 18342287
The FCRL3 -169T>C polymorphism is associated with rheumatoid arthritis and shows suggestive evidence of involvement with juvenile idiopathic arthritis in a Scandinavian panel of autoimmune diseases.
Ann Rheum Dis 2007 Dec. Epub 2007 des 7
PMID: 18065500
Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis.
Hum Immunol 2007 Sep;68(9):748-55. Epub 2007 jun 28
PMID: 17869649
Genetic screening of Scandinavian families with febrile seizures and epilepsy or GEFS+.
Acta Neurol Scand 2008 Apr;117(4):289-92. Epub 2007 okt 10
PMID: 17927801
Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease.
Hum Immunol 2007 Jul;68(7):592-8. Epub 2007 apr 13
PMID: 17584581
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.
N Engl J Med 2007 Jan;356(3):237-47.
PMID: 17229951
The effect of red wine on plasma leptin levels and vasoactive factors from adipose tissue: a randomized crossover trial.
Alcohol Alcohol 2007 Nov-Dec;42(6):525-8. Epub 2007 aug 1
PMID: 17670801
Anthocyanins inhibit nuclear factor-kappaB activation in monocytes and reduce plasma concentrations of pro-inflammatory mediators in healthy adults.
J Nutr 2007 Aug;137(8):1951-4.
PMID: 17634269
A daily glass of red wine induces a prolonged reduction in plasma viscosity: a randomized controlled trial.
Blood Coagul Fibrinolysis 2006 Sep;17(6):471-6.
PMID: 16905951
A twin study of nitric oxide levels measured by serum nitrite/nitrate.
Twin Res Hum Genet 2006 Apr;9(2):210-4.
PMID: 16611490
siRNA: a potential tool for future breast cancer therapy?
Crit Rev Oncog 2006 Jul;12(1-2):127-50.
PMID: 17078209
CFTR gene mutations and asthma in the Norwegian Environment and Childhood Asthma study.
Respir Med 2006 Dec;100(12):2121-8. Epub 2006 mai 5
PMID: 16678395
En ny æra for DNA-sekvensering - nye muligheter og nye utfordringer i humanmedisin.
Genialt 1/2010 s. 16-18
Asthma and allergy in childhood: genetics of the inflammatory reaction.
- Disputert:
- desember 2007
- Hovedveileder:
- Karin Lødrup Carlsen
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